Taiwan FDA registration 7143fd14d044f9360383f88bb278665a
“Keystone” Endosseous Dental Implant Accessories (Non-Sterile)
TW: “金石”牙齒骨內植入物附件 (未滅菌)
Taiwan·Risk Class 1·MD·KEYSTONE DENTAL, INC.·Registered May 28, 2014 – May 28, 2024ExpiredRegistration details
- Analysis ID
- 7143fd14d044f9360383f88bb278665a
- License Form
- Ministry of Health Medical Device Import No. 014178
- Customs Code
- DHA09401417801
Company information
- Manufacturer
- KEYSTONE DENTAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HUNG KUO MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3980 Dental Intraosseous Implant Attachment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 28, 2014
- Expiry Date
- May 28, 2024
About this record
Access comprehensive regulatory information for “Keystone” Endosseous Dental Implant Accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7143fd14d044f9360383f88bb278665a and manufactured by KEYSTONE DENTAL, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..
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